|Publication number||US6572993 B2|
|Application number||US 09/742,757|
|Publication date||Jun 3, 2003|
|Filing date||Dec 20, 2000|
|Priority date||Dec 20, 2000|
|Also published as||DE10160545A1, US20020076588|
|Publication number||09742757, 742757, US 6572993 B2, US 6572993B2, US-B2-6572993, US6572993 B2, US6572993B2|
|Inventors||Prabhakar Singh, Mehrdad Teimor, Walter Franklin Clark|
|Original Assignee||Visteon Global Technologies, Inc.|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (13), Referenced by (10), Classifications (13), Legal Events (4)|
|External Links: USPTO, USPTO Assignment, Espacenet|
The present invention relates generally to fuel cell systems and more particularly to fuel cell systems with controlled anode exhaust.
Fuel cell systems currently being developed for power generation applications operate on basically the same electrochemical principles as a battery system to generate electricity. Fuel cell systems generally consist of a reformer, a fuel cell stack, and an power converter (generator).
In a typical power generation system, first the reformer, or fuel processor, converts a feedstock, typically a hydrocarbon fuel such as gasoline or natural gas, into a hydrogen rich gas. Many types of reformers can be used to convert the feedstock, including steam reformers, auto thermal reformers, partial oxidation reformers, preferential oxidation reformers, and high and low temperature shift processing reformers.
Next, the hydrogen gas stream is removed from the reformer and fed into an anode chamber of a fuel cell stack for electrochemical oxidation. In this step, the hydrogen rich gas is oxidized in the presence of a catalyst contained on the walls of the anode chamber to form hydrogen protons and electrons. An electrolytic membrane allows the hydrogen protons to enter a cathode chamber, where the hydrogen protons react with oxygen from air to form water and heat that is released from the cathode chamber into the atmosphere. The electrons within the cathode chamber exit the fuel cell along an external remote load wire and are converted by the generator to usable power. By stacking a few hundred fuel cells together to form a fuel cell stack, the amount of power generated can be substantially increased. Unoxidized fuel within the anode chamber exits the fuel cell and enters a combuster for burning.
During normal operating conditions, wherein the electrical load demand on the fuel cell remains relatively steady, the oxidation reaction efficiency of the fuel cell is relatively constant at approximately 80-90%. The amount of unoxidized fuel thus entering the combuster therefore remains relatively constant, and as such the combuster temperature that is a function of the amount of unoxidized fuel burned within the combuster is maintained within an acceptable range.
However, under transient operating conditions, wherein the electrical load demand on the fuel cell could be decreased, the amount of unoxidized fuel within the anode chamber substantially increases. Burning of this excess unoxidized fuel in the combuster leads to the generation of high temperatures and accelerated corrosion (or melting) of the combuster material. Such temperature transients in the combuster require expensive construction materials and higher quality insulation to provide thermal stability in the combuster. Combustion of the unoxidized fuel in the combuster also reduces the overall fuel system efficiency.
Another alternative is to recycle the unoxidized fuel through the inlet anode gas stream of the fuel cell. However, recycling and injection of hydrogen depleted tail gas in the anode gas stream leads to increased parasitic power loss.
It is thus highly desirable to control the temperature in the combuster by improving the electrochemical oxidation of the fuel within the fuel cell during transient load conditions.
The present invention overcomes the above identified deficiencies of presently available fuel cell systems by providing a means for oxidizing heated reformed fuel gas in a fuel cell during transient load conditions. Electrochemical oxidation of the fuel in the fuel cell minimizes or prevents a buildup of anode gas in the anode chamber. Also, combustion of unoxidized gas is minimized in the combuster, thereby preventing excess heat buildup in the combuster that could damage the fuel processing assembly.
The above objects are accomplished by providing a methodology for operating a fuel cell power generation system in conjunction with an energy storage system in a parallel mode operation to prevent transient increases in the combustion of anode gas during changes in electrical load demand. The energy storage device consists of either a battery pack or a bank of capacitors/super capacitors that are attached in parallel to the fuel cell system such that both can provide power during normal and/or transient operations. Normally unoxidized reformed gas within the anode chamber during transient conditions is oxidized and the electrical energy created by the oxidation stored in an energy storage device. This prevents the discharge of larger than normal amounts of reformer gas to the combuster, gas that normally results in very high temperature combustion within the combuster (approximately 1400-1500 degrees Celsius) that can cause corrosion (or melting) of combuster material or otherwise damage to the fuel processing assembly.
Other objects and advantages of the present invention will become apparent upon considering the following detailed description and appended claims, and upon reference to the accompanying drawings.
FIG. 1 is a schematic representation of a fuel cell power generation system having an energy storage device according to the preferred embodiment of the present invention;
FIG. 2 is a graphical representation of how the power levels, anode exhaust levels, and combuster temperature change relative to time in transient load conditions in a fuel cell power generation system without an energy storage device;
FIG. 3 is a graphical representation of how the power levels, anode exhaust levels, and combuster temperature change relative to time in transient load conditions in a fuel cell power generation system with an energy storage device of FIG. 1, wherein the fuel cell power generation system is idealized; and
FIG. 4 is a graphical representation of how the power levels, anode exhaust levels, and combuster temperature change relative to time in transient load conditions in a fuel cell power generation system with an energy storage device of FIG. 1, wherein the fuel cell power generation system is not idealized.
The present invention describes a methodology of operating a fuel cell power generation system in conjunction with an energy storage system in a parallel mode operation to prevent transient increases in the combustion of anode gas during changes in the electrical load demand.
Referring now to FIG. 1, a fuel processing assembly 10 is depicted. The assembly 10 includes a heat exchange reformer 12 for converting hydrocarbon fuels into a reformed gas stream that is used by electrochemical fuel cells 30 to generate electricity. The reformer 12 has an intake port 20 for receiving feed gas, typically gasoline, natural gas, or some other type of hydrocarbon, from a reservoir (not shown) and an outlet port 22 for removing the processed reformed feed gas from the reformer 12. The feed gas may also comprise any combination of water, oxygen, nitrogen, carbon monoxide, carbon dioxide, and hydrogen. The feed gas is processed into a reformed gas within the reformer 12. Processes used to convert the feed gas into the reformed gas include steam reforming, auto thermal reforming, partial oxidation, preferential oxidation, high temperature shift processing, low temperature shift processing, or some other type of processing that is known in the art. In addition, the reformer 12 has a burner inlet port 24 from fuel cell 30 for receiving heated burner exhaust gas and/or a partially or wholly unreacted mixture of fuel and oxidant (hereinafter referred to as burner exhaust gas). The reformer 12 also has a burner outlet port 26 for removing cooled burner exhaust gas from the reformer 12. The reformer 12 may also contain a high temperature/low temperature shift reactor (not shown) and/or a preferential reactor (not shown) for converting carbon monoxide gas to carbon dioxide in a method that is known in the art. Ideally, the reform gas leaving the reformer 12 will contain less than 10 parts per million (ppm) carbon monoxide. This is important for two reasons. First carbon monoxide is undesirable to release into the atmosphere. Second, carbon monoxide may react within the fuel cell 30 to coat the fuel cell catalyst that is used to facilitate reactions during the oxidation process, and thus excess carbon monoxide will limit the efficiency of the fuel cell 30 over time.
Processed reform gas, typically hydrogen or some hydrogen rich gas, exits the outlet port 22 and enters the anode inlet 32 into an anode chamber 33 of an electrochemical fuel cell 30. A series of individual electrochemical fuel cells 30 form a fuel cell stack 31. A catalyst (not shown) coated on the walls of the anode chamber 33 of the electrochemical fuel cell 30 oxidizes the hydrogen atoms into electrons and protons. The electrons escape through a wire 36 coupled to the electrochemical fuel cell to a generator 38. The hydrogen protons travel through an electrolyte membrane 34 to a cathode chamber 39 and combine with oxygen that is fed into the cathode inlet 40 of the electrochemical fuel cell 30 to form water and heat (which are the only emissions products if pure hydrogen is used as the input gas feed) that are expelled from the electrochemical cells 30 through outlet ports 42, 44.
Under normal operating conditions, the oxidation of reform gas is approximately 80-90% complete. Unoxidized reform gas then exits the anode chamber 33 via the anode outlet 46 and enters a combuster 50 for burning. The unoxidized reform gas is converted to carbon dioxide and water within the combuster, ideally at between 500-900 degrees Celsius, in a process that is well known in the art.
During transient operating conditions, a condition that occurs when the electrical load on the electrochemical fuel cell 30 changes based on load demand, the reform gas is typically allowed to exit the anode chamber 33 through outlet 46 without electrochemical oxidation (utilization) in much greater quantities. This is done to minimize the buildup of reform gas within the anode chamber 33, a condition that may damage the fuel cell 30. This reform gas may then be recirculated through the cell 30 or is allowed to enter the combuster 50. In the former case, this recycling and injection of hydrogen depleted tail gas leads to increased parasitic power loss. In the latter case, burning of fuel in the combuster 50 increases the combuster temperatures and may accelerate the corrosion of combuster material. This can lead to reduced fuel cell system efficiency. The increased temperatures within the combuster 50 for example may reach as high as 1400-1500 degrees Celsius during transient load conditions.
To help to alleviate these problems, an energy storage device 80 is attached in parallel to the fuel cell 30. The energy storage device 80 may be a battery pack, a bank of capacitors (or super capacitors) or other storage devices or combinations thereof. The energy storage device 80 provides power during normal or transient operations. The energy storage device 80 is allowed to maintain a power capacity, or charge level, at a predetermined level during nominal operation less than the maximum charge level. During electrical load transition, or transient load conditions, the excess unoxidized (unreacted) reform gas within the anode chamber 33 that would normally be discharged to the combuster 50 in large amounts is instead electrochemically oxidized to charge the energy storage device 80 towards full capacity. The size and charge level of the energy storage device 80 is a sized to maintain the percentage of unoxidized fuel discharging the anode chamber 33 to the combuster 50 at a nearly uniform level. In a preferred embodiment, the charge level is maintained at approximately 80% of full capacity.
After normalization of the fuel flow and load demand in the anode chamber 33, the energy storage device 80 may slowly discharge the excess charge to the predetermined charge level to allow for additional charge to be accepted during the transient period. Both the fuel processing assembly 10 and energy storage device 80 can be operated continuously or the energy storage device 80 can be operated intermittently to maintain the charge level.
FIGS. 2-4 compare fuel cell generation power systems both with and without the energy storage device for changes in power levels, unoxidized anode exhaust volume, combuster temperature, and energy storage device power levels before, during and after a transient load condition. These are depicted on lines 101, 103, 105, and 107 respectively. In FIG. 3, the energy storage device is assumed to be capable of continually storing energy during the entire transient load event, and thus the flow of anode gas entering the fuel cell remains constant. In FIG. 4, the flow of anode gas entering the fuel cell is controlled using a controller, and hence the storage of energy by the energy storage device fluctuates during the course of the transient load event.
As seen in FIG. 2, during transient electrical load, as depicted between times 100 and 112, the power level along line 101 drops to a transient load condition. Processed reformer gas contained within the anode chamber 33 and peripheral volume does not chemically oxidize, and thus the level of unoxidized fuel exiting the anode chamber 33 to the combuster 50 correspondingly increases, as depicted on line 103. Fuel rich gas entering the combuster 50 raises the temperature within the combuster 50, as is depicted on line 105. These elevated temperatures may damage various components of the combuster 50 and fuel cell power generation system.
In the present invention, as seen in FIG. 3, during transient electrical load conditions reformer gas contained within the anode chamber 33 is allowed to electrochemically oxidize and electrical power generated is stored in the energy storage device 80. This is depicted by the increase in energy along line 107. This prevents the buildup of the unoxidized gas within the anode chamber 33 that subsequently enters the combuster 50, which is depicted along line 103. Also, combustion temperatures within the combuster 50 are maintained at levels similar to normal operating conditions as shown on line 105. The amount of reformer gas entering the anode chamber 33 from the reformer 12 is held constant during both normal and transient load conditions.
Referring now to FIG. 4, the amount of unoxidized gas entering the anode chamber is lessened at time 100 in response to the transient load condition. As this condition is not idealized, as in FIG. 3, there is typically a lag between the time the controllers (not shown) direct that the amount of unoxidized gas entering the anode chamber is lessened and the actual lessening of the amount of unoxidized fuel entering the anode chamber 33. Thus, along line 107, the energy storage device 80 will absorb the excess energy until time 102. At time 102, the amount of unoxidized gas entering the anode chamber 33 is lowered to a level sufficient not to require the energy storage device 80 to be necessary. Thus, at time 102, the energy storage device 80 dissipates the excess energy back to its original predetermined level at time 104. Similarly, at time event 112, wherein the electrical load demand is stepped back up to normal levels, there is not enough unoxidized fuel within the anode chamber to support the change, hence the energy storage device 80 provides the excess energy necessary to maintain the generator at the power level desired. This corresponds to the dip in energy storage power level from time 112 to 114. As the controller directs more unoxidized fuel to enter the anode chamber 33, the storage level of electrical power in the energy storage device 80 can be returned to its normal level as depicted at time 116.
The energy storage device 80 serves many important functions. First, the energy storage device prevents the buildup of excessive quantities of unoxidized fuel in the anode chamber 33 during transient load conditions, fuel that ultimately may damage the combuster 50.
Second, the energy storage device functions as a reserve energy source in times where more electrical power may be required by the system. Most importantly, the addition of an energy storage device 80 functions to maintain the amount of unoxidized fuel entering the combuster 50 during transient load conditions to levels approximately the same as in normal operating conditions. In this way, the combuster 50 temperature is maintained within an acceptable temperature range preferably between 500 and 900 degrees Celsius. Ultimately, this protects the life of the combuster 50 and fuel cell 30 without the use of expensive material within the combuster or fuel processing assembly 10.
While the invention has been described in terms of preferred embodiments, it will be understood, of course, that the invention is not limited thereto since modifications may be made by those skilled in the art, particularly in light of the foregoing teachings.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US5401589 *||Nov 22, 1991||Mar 28, 1995||Vickers Shipbuilding And Engineering Limited||Application of fuel cells to power generation systems|
|US5969435 *||Mar 19, 1997||Oct 19, 1999||Nextek Power Systems, Inc.||Modular DC cogenerator systems|
|US6077620 *||Nov 26, 1997||Jun 20, 2000||General Motors Corporation||Fuel cell system with combustor-heated reformer|
|US6159626 *||Jul 6, 1999||Dec 12, 2000||General Motors Corporation||Fuel cell system logic for differentiating between rapid and normal shutdown commands|
|US6232005 *||Nov 20, 1997||May 15, 2001||General Motors Corporation||Fuel cell system combustor|
|US6268074 *||Apr 5, 1999||Jul 31, 2001||General Motors Corporation||Water injected fuel cell system compressor|
|US6306531 *||May 5, 2000||Oct 23, 2001||General Motors Corporation||Combustor air flow control method for fuel cell apparatus|
|US6316134 *||Sep 13, 1999||Nov 13, 2001||Ballard Generation Systems, Inc.||Fuel cell electric power generation system|
|US6380637 *||Jul 8, 1999||Apr 30, 2002||Ztek Corporation||Off-board station and an electricity exchanging system suitable for use with a mobile vehicle power system|
|US6391484 *||Jul 6, 1999||May 21, 2002||General Motors Corporation||Fuel processor temperature monitoring and control|
|US6410175 *||Nov 12, 1998||Jun 25, 2002||Ballard Power Systems Inc.||Fuel cell system with improved starting capability|
|US6416893 *||Feb 11, 2000||Jul 9, 2002||General Motors Corporation||Method and apparatus for controlling combustor temperature during transient load changes|
|US6436561 *||May 5, 2000||Aug 20, 2002||General Motors Corporation||Methanol tailgas combustor control method|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US6991864||Sep 23, 2003||Jan 31, 2006||Utc Fuel Cells, Llc||Storage of fuel cell energy during startup and shutdown|
|US7659018 *||Nov 16, 2001||Feb 9, 2010||Honda Giken Kogyo Kabushiki Kaisha||Fuel cell power control unit|
|US7790303||Nov 14, 2005||Sep 7, 2010||Utc Power Corporation||Storage of fuel cell energy during startup and shutdown or other power transitions|
|US7955746||Jul 16, 2010||Jun 7, 2011||Utc Power Corporation||Storage of fuel cell energy during startup and shutdown or other power transitions|
|US20050064258 *||Sep 23, 2003||Mar 24, 2005||Fredette Steven J.||Storage of fuel cell energy during startup and shutdown|
|US20060068249 *||Nov 14, 2005||Mar 30, 2006||Fredette Steven J||Storage of fuel cell energy during startup and shutdown or other power transitions|
|US20070020491 *||Jul 21, 2005||Jan 25, 2007||Michael Ogburn||Stoichiometric control methodology for fuel cell systems|
|US20130108895 *||May 2, 2013||Plug Power Inc.||Method to control current in a fuel cell system|
|WO2005053061A2||Nov 17, 2004||Jun 9, 2005||Utc Fuel Cells Llc||Electric storage augmentation of fuel cell system transient response|
|WO2013006427A1 *||Jun 29, 2012||Jan 10, 2013||Sun Catalytix Corporation||Methods and systems useful for solar energy storage|
|U.S. Classification||429/423, 429/442, 429/444|
|International Classification||H01M8/04, H01M16/00, H01M8/06|
|Cooperative Classification||Y02E60/50, H01M8/0662, H01M16/003, H01M8/04|
|European Classification||H01M16/00F, H01M8/06C, H01M8/04|
|Dec 20, 2000||AS||Assignment|
|Dec 20, 2006||REMI||Maintenance fee reminder mailed|
|Jun 3, 2007||LAPS||Lapse for failure to pay maintenance fees|
|Jul 24, 2007||FP||Expired due to failure to pay maintenance fee|
Effective date: 20070603